Qureshi Adnan I, Ishfaq Ammad, Ishfaq Muhammad F, Pandhi Abhi, Ahmed Sundas I, Singh Savdeep, Kerro Ali, Krishnan Rashi, Deep Aman, Georgiadis Alexandros L
Zeenat Qureshi Stroke Institute, St. Cloud, MN, USA.
University of Tennessee Health Science Center, Memphis, TN, USA.
J Vasc Interv Neurol. 2018 Nov;10(2):33-40.
To assess the effectiveness of cilostazol, a selective inhibitor of phosphodiesterase type III, in preventing cerebral ischemia related to cerebral vasospasm after aneurysmal subarachnoid hemorrhage (SAH).
A total of six clinical studies met the inclusion criteria and were included in the meta-analysis. We calculated pooled risk ratios (RR) and 95% confidence intervals (CI) using random-effects models. The primary endpoint was cerebral ischemia related to vasospasm. Secondary endpoints were angiographic vasospasm, new cerebral infarct, mortality, and death or disability at the final follow-up.
A total of 136 (22%) of 618 subjects (38 and 98 assigned to cilostazol and control treatments, respectively) with SAH developed cerebral ischemia related to vasospasm. The risk of cerebral ischemia related to vasospasm was significantly lower in subjects assigned to cilostazol treatment ( 0.43; 95% CI 0.31-0.60; < 0.001). The risks of angiographic vasospasm ( 0.67, 95% CI 0.54-0.84, < 0.001 ) and new cerebral infarct ( 0.37, 95% CI 0.24-0.57, < 0.001) were significantly lower in subjects assigned to cilostazol treatment. There was a significantly lower rate of death or disability in subjects assigned to cilostazol treatment at follow-up ( 0.55, 95% 0.39-0.78, = 0.001).
The reduction in rates of cerebral ischemia related to vasospasm and death or disability at follow-up support further evaluation of oral cilostazol in patients with aneurysmal SAH in a large randomized clinical trial.
评估III型磷酸二酯酶选择性抑制剂西洛他唑预防动脉瘤性蛛网膜下腔出血(SAH)后与脑血管痉挛相关的脑缺血的有效性。
共有六项临床研究符合纳入标准并纳入荟萃分析。我们使用随机效应模型计算合并风险比(RR)和95%置信区间(CI)。主要终点是与血管痉挛相关的脑缺血。次要终点是血管造影血管痉挛、新的脑梗死、死亡率以及最后随访时的死亡或残疾情况。
618例SAH患者中共有136例(22%)(分别有38例和98例分配至西洛他唑治疗组和对照组)发生了与血管痉挛相关的脑缺血。分配至西洛他唑治疗组的患者发生与血管痉挛相关的脑缺血的风险显著更低(0.43;95%CI 0.31 - 0.60;<0.001)。分配至西洛他唑治疗组的患者发生血管造影血管痉挛(0.67,95%CI 0.54 - 0.84,<0.001)和新的脑梗死(0.37,95%CI 0.24 - 0.57,<0.001)的风险也显著更低。在随访时,分配至西洛他唑治疗组的患者死亡或残疾率显著更低(0.55,95%CI 0.39 - 0.78,P = 0.001)。
与血管痉挛相关的脑缺血发生率以及随访时的死亡或残疾率降低,支持在大型随机临床试验中对动脉瘤性SAH患者进一步评估口服西洛他唑。